# A Handy and Visual Detection Method for Potato Late Blight Utilizing Multi-Copy Specific Sequences and RPA-LFD Technology

**Authors:** Yi Que, RongSheng Wang, Li Sheng, ZhiWei Zhang, Xia Wang, Lei Chen, GuangJin Fan

PMC · DOI: 10.4014/jmb.2509.09040 · 2026-02-12

## TL;DR

This study introduces a fast and sensitive detection method for potato late blight using a new DNA sequence and RPA-LFD technology, enabling early diagnosis without specialized equipment.

## Contribution

A novel multi-copy DNA sequence (SSPI1) and a rapid RPA-LFD detection method for potato late blight with high sensitivity and specificity.

## Key findings

- SSPI1 offers higher sensitivity than PiYPT1 and improved specificity over PiITS in PCR assays.
- The RPA-LFD method can detect potato late blight in 35 minutes with a detection limit of 11 copies/μl.
- The method successfully detects infections in asymptomatic leaves under field conditions.

## Abstract

Potato late blight, caused by Phytophthora infestans, is one of the most destructive diseases affecting global potato production. Rapid and accurate detection of the pathogen is essential for effective disease prevention and control. In this study, a novel multi-copy and specific DNA sequence, designated SSPI1 (Specific Sequence of Phytophthora infestans 1), was identified through bioinformatic analysis. Using seven closely related Phytophthora species and two additional common potato pathogens as controls, PCR assays demonstrated that SSPI1 offers higher sensitivity than PiYPT1 and improved specificity over PiITS. Based on this novel multi-copy sequence, we developed a rapid, user-friendly, and highly sensitive detection method for potato late blight by combining recombinase polymerase amplification (RPA) with lateral flow dipstick (LFD) technology. The entire diagnostic process—including crude DNA extraction, RPA amplification, and visual detection—can be completed within 35 min without the need for specialized equipment. Optimization results indicated that among nine candidate RPA primer pairs, RPA-F1/RPA-R2 exhibited the highest amplification efficiency. The optimal RPA reaction temperature range was determined to be 27–42°C, with a detection limit of 11 copies/μl for SSPI1. This method could detect as little as 100 pg of genomic DNA, identify samples collected as early as 24 h post-inoculation, and even detect infections in asymptomatic leaves under field conditions, demonstrating superior sensitivity compared to the PiYPT1-targeted RPA-LFD assay. Overall, this study presents a highly sensitive, specific, practical, and efficient tool for the early and rapid detection of potato late blight.

## Linked entities

- **Species:** Phytophthora infestans (taxon 4787)

## Full-text entities

- **Diseases:** soil-borne disease (MESH:D005242), P. infestans infections (MESH:D007239), LFD (MESH:D054318), late blight (MESH:D000067562)
- **Chemicals:** agarose (MESH:D012685), chloroform (MESH:D002725), CQ (MESH:C048021), GZ (-), water (MESH:D014867), NaOH (MESH:D012972), Magnesium Acetate (MESH:C000656591), Biotin (MESH:D001710), phosphate (MESH:D010710), FAM (MESH:C031179)
- **Species:** Ralstonia solanacearum (species) [taxon 305], Pythium (genus) [taxon 4797], Solanum tuberosum (potatoes, species) [taxon 4113], Phytophthora nicotianae (black shank of tobacco agent, species) [taxon 4792], Phytophthora palmivora (species) [taxon 4796], Alternaria solani (species) [taxon 48100], Phytophthora heveae (species) [taxon 129351], Phytophthora sojae (species) [taxon 67593], Phytophthora cactorum (species) [taxon 29920], Sarcoptes scabiei (species) [taxon 52283], Anaplasma phagocytophilum (agent of human granulocytic ehrlichiosis, species) [taxon 948], Nicotiana tabacum (American tobacco, species) [taxon 4097], Phytophthora cinnamomi (species) [taxon 4785], Phytophthora capsici (species) [taxon 4784], Phytophthora infestans (potato late blight agent, species) [taxon 4787]
- **Cell lines:** T30-4 — Homo sapiens (Human), Transformed cell line (CVCL_B4J9)

## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12975500/full.md

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Source: https://tomesphere.com/paper/PMC12975500